A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5465963



Internal ID243814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:37659702..37660325hg38UCSC Ensembl
chr4:37661324..37661947hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38624
hg19624
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16947414
Samples
Known GenesRELL1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5465963
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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